1,3,2-Dioxaborolane, 2,2'-[[(1E)-1,2-diphenyl-1,2-ethenediyl]di-4,1-phenylene]bis[4,4,5,5-tetramethyl-

≥98%

Reagent Code: #98386
fingerprint
CAS Number 1260865-88-0

science Other reagents with same CAS 1260865-88-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 584.35968 g/mol
Formula C₃₈H₄₂B₂O₄
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This chemical is primarily utilized in organic synthesis, particularly as a key intermediate in the preparation of conjugated polymers and organic electronic materials. Its structure, featuring boronate ester groups, makes it highly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, it is used in the development of organic light-emitting diodes (OLEDs) and photovoltaic devices due to its ability to facilitate the creation of highly efficient and stable organic semiconductors. Its application extends to the field of materials science, where it contributes to the design of advanced materials with tailored electronic properties.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance colorless to white
Purity 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,450.00
inventory 500mg
10-20 days ฿8,020.00
inventory 1g
10-20 days ฿13,100.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
1,3,2-Dioxaborolane, 2,2'-[[(1E)-1,2-diphenyl-1,2-ethenediyl]di-4,1-phenylene]bis[4,4,5,5-tetramethyl-
No image available

This chemical is primarily utilized in organic synthesis, particularly as a key intermediate in the preparation of conjugated polymers and organic electronic materials. Its structure, featuring boronate ester groups, makes it highly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, it is used in the development of organic light-emitting diodes (OLEDs) and photovoltaic devices due to

This chemical is primarily utilized in organic synthesis, particularly as a key intermediate in the preparation of conjugated polymers and organic electronic materials. Its structure, featuring boronate ester groups, makes it highly valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, it is used in the development of organic light-emitting diodes (OLEDs) and photovoltaic devices due to its ability to facilitate the creation of highly efficient and stable organic semiconductors. Its application extends to the field of materials science, where it contributes to the design of advanced materials with tailored electronic properties.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...